In Hospital 24 Hour Observation of Syncope Patients

Recruiting Observational Study
Syncope
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
640 (estimated)
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Other
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About This Trial
Syncope is very common and has a broad differential diagnosis. Guidelines on syncope recommend to apply guideline based syncope algorithm (SA) to identify low- / intermediate risk syncope patients and recommend to discharge these patients. The time window when to discharge these patients is not defined in the guidelines. In current medical practice low- / intermediate risk syncope patients are eit…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: All patients that are assessed as low- and intermediate risk syncope, are eligible for inclusion in this trial. The initial syncope evaluation includes: 1. Complete and thorough history taking of the syncope event and past medical history 2. Physical examination including supi…
Contacts

Frederik de Lange, MD PhD

+31 (0) 20 5669111

f.j.delange@amsterdamumc.nl

CONTACT

Elise Hulsman, RN

e.l.hulsman@amsterdamumc.nl

CONTACT